CooperSurgical recalls Oxygen Sensor Model K54019-2 used in G185 & G210 Incubators and G603 Work Chambers. Sensors may display incorrect oxygen levels, risking embryo loss during storage.
Units are displaying output readings that differ from the measurements taken using a Gas Analyzer. When the display is reading a target setting of 5%, an external meter is reading between 3% and 12% and the Incubator does not alarm. May result in loss of embryo during storage.
CooperSurgical is recalling Oxygen Sensor Model K54019-2 used in certain incubators and work chambers. These sensors may show inaccurate oxygen readings, which could lead to embryo loss during storage if not corrected.
The sensors may display oxygen readings that differ significantly from external gas analyzers. When the display shows 5% oxygen, external meters read between 3% and 12%. This can cause the incubator to fail to alarm, potentially leading to embryo loss during storage.
Users of G185, G210, and G603 incubators/work chambers with the specific oxygen sensor model. Most at risk are laboratory or embryology staff handling embryos.
Check if your incubator or work chamber has the Oxygen Sensor Model K54019-2. Look for the serial numbers listed in the recall (e.g., 531540-531700, 532001, etc.) or part numbers like K22400-110, K59500, etc.
Identify if your incubator or work chamber has the listed serial numbers (e.g., 531540-531700, 532001, etc.) or part numbers like K22400-110, K59500.
The Oxygen Sensor Model K54019-2 used in G185, G210, and G603 incubators/work chambers.
Check if your incubator or work chamber has the listed serial numbers (e.g., 531540-531700, 532001, etc.) or part numbers like K22400-110, K59500.
The sensor may display incorrect oxygen readings, which could lead to embryo loss during storage if the incubator fails to alarm.
We’ve drafted a message you can send CooperSurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-2307-2021 — CooperSurgical CooperSurgical Hello, I own a CooperSurgical that is covered by recall Z-2307-2021 from CooperSurgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
